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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661086Generated: October 30, 2026

Ethyl Acetate → HCID 67429319, compound

https://huagongshe.com/reaction/1661086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-HeptanamineHCID 38665—
ReactantMethyl 2-amino-5-chloro-3-iodobenzoateHCID 7020924—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
ProductHCID 67429319HCID 67429319315.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

Added successively to a solution of 3 g of methyl 2-amino-5-chloro-3-iodobenzoate in 100 cm3 of toluene, under an inert atmosphere and at a temperature close to 20° C., are 2.2 g of 4-aminoheptane then 12 cm3 of a 2M solution of trimethylaluminum in toluene. The reaction mixture is heated, while stirring, for 16 h at 100° C., then it is cooled to 20° C. in order to then be poured over a mixture of 250 g of water/ice and 150 cm3 of ethyl acetate. The suspension obtained is filtered over a Celite 545 pellet. The aqueous phase is extracted with 3 lots of 100 cm3 of ethyl acetate. The organic phases are combined then washed with 100 cm3 of a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated using a rotary evaporator under reduced pressure (5 kPa). The 12 g of crude product obtained are purified by flash chromatography over silica (column: 200 g; particle size: 15-40 μm; eluent: 100% dichloromethane). After concentrating the fractions under reduced pressure, 3.21 g of 2-amino-5-chloro-3-iodo-N-(1-propylbutyl)benzamide are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030320B2
Source datasetuspto-grants-2011_10
ORD IDord-286cce72862a425795c087c17a591759
Source noteuspto-grants-2011_10